A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149731



Internal ID15878347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14982570..14995156hg38UCSC Ensembl
Innerchr17:14885887..14898473hg19UCSC Ensembl
Innerchr17:14826612..14839198hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3812587
hg1912587
hg1812587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574426
Supporting Variants
SamplesHGDP01185
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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